Clinical Research Coordinator
West Haven, CTContractor
Behavioral Health Market Context
Apply Nowvia BrightMove
Job Description
inations. Reviews, in real-time, all laboratory and relevant clinical reports. Implements appropriate medical interventions for significant findings found during study participant evaluations. Ensures that all study participants have appropriate emergency medical access. Reports all significant medical events in study participants appropriately. Perform activities related to consenting, screening, enrollment, and perform follow up of study participants, including attention to safety assessment and reporting while hospitalized and during follow up of study participants. Ensure protocol and Protocol Implementation Modules (PIMs) are followed and compliance with GCP, OHRP and FDA requirements.
Who You Will Work With
Collaborate with other health care professionals and service providers to ensure optimal patient care.
Who You Are
An experience Research Coordinator.
Our minimum requirements for this role:
Required
· Graduate from an accredited school in health-related field required.
· Nursing License not required but prefer Certified Clinical Research Professional (CCRP) or LVN/RN
· 2-5 years of experience in a clinical research setting with protocols and clinical trials
· Expertise in the fundamentals of clinical trials
· Previous experience in clinical data management, database operations and analysis
· Certified in GCP
· Experience with IRB and FDA requirements
· CPR Certification (American Heart Association)
· GCP Training is required
· HSP (Human Subjects Protection) Training is required
· Position is subject to approved background check
Current Employee Testimonies
Best work experience to date. The salary and benefits are excellent, while the company cares about its employees. It’s rare when the CEO knows each employee personally.
About Your New Company
Employment with DTI means growth. DTI is a Baltimore-based certified HUBZone business providing complex mission-critical IT and Health solutions. Valuing Ethics Expertise, Technology and Delivery of Superior Service.
Who You Will Work With
Collaborate with other health care professionals and service providers to ensure optimal patient care.
Who You Are
An experience Research Coordinator.
Our minimum requirements for this role:
Required
· Graduate from an accredited school in health-related field required.
· Nursing License not required but prefer Certified Clinical Research Professional (CCRP) or LVN/RN
· 2-5 years of experience in a clinical research setting with protocols and clinical trials
· Expertise in the fundamentals of clinical trials
· Previous experience in clinical data management, database operations and analysis
· Certified in GCP
· Experience with IRB and FDA requirements
· CPR Certification (American Heart Association)
· GCP Training is required
· HSP (Human Subjects Protection) Training is required
· Position is subject to approved background check
Current Employee Testimonies
Best work experience to date. The salary and benefits are excellent, while the company cares about its employees. It’s rare when the CEO knows each employee personally.
About Your New Company
Employment with DTI means growth. DTI is a Baltimore-based certified HUBZone business providing complex mission-critical IT and Health solutions. Valuing Ethics Expertise, Technology and Delivery of Superior Service.
Qualifications
- •An experience Research Coordinator
- •Graduate from an accredited school in health-related field required
- •Nursing License not required but prefer Certified Clinical Research Professional (CCRP) or LVN/RN
- •2-5 years of experience in a clinical research setting with protocols and clinical trials
- •Expertise in the fundamentals of clinical trials
- •Previous experience in clinical data management, database operations and analysis
- •Certified in GCP
- •Experience with IRB and FDA requirements
- •CPR Certification (American Heart Association)
- •GCP Training is required
- •HSP (Human Subjects Protection) Training is required
- •Position is subject to approved background check
Benefits
- •The salary and benefits are excellent, while the company cares about its employees
Responsibilities
- •Work with site personnel to conduct COIVD-19 therapeutic clinical research studies
- •Performs protocol-mandated initial and follow-up medical histories and physical examinations
- •Reviews, in real-time, all laboratory and relevant clinical reports
- •Implements appropriate medical interventions for significant findings found during study participant evaluations
- •Ensures that all study participants have appropriate emergency medical access
- •Reports all significant medical events in study participants appropriately
- •Perform activities related to consenting, screening, enrollment, and perform follow up of study participants, including attention to safety assessment and reporting while hospitalized and during follow up of study participants
- •Ensure protocol and Protocol Implementation Modules (PIMs) are followed and compliance with GCP, OHRP and FDA requirements
- •Collaborate with other health care professionals and service providers to ensure optimal patient care
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